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Roll-A-Set

by Steris Corporation 6 variants

Roll-A-Set (850010) is a Class I device made by Steris Corporation, listed in FDA GUDID since 31 Mar 2021 (UDI-DI 10724995021488), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10724995021488 UDI-DI Date31 Mar 2021ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Surgical instrument guard, single-use, sterile
Model / Ref / Catalog
Roll-A-Set, 850010
Primary DI / UDI-DI
10724995021488
FDA product code
MDM
GMDN term
Surgical instrument guard, single-use, sterile
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical instrument guard, single-use, sterile

Similar devices

Other devices filed under FDA product code MDM (INSTRUMENT, MANUAL, SURGICAL, GENERAL USE).

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)